ZMP
slc2a8
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 2, facilitated glucose transporter member 8 [Source:RefSeq peptide;Acc:NP_997
Human Orthologue:
SLC2A8
Human Description:
solute carrier family 2 (facilitated glucose transporter), member 8 [Source:HGNC Symbol;Acc:13812]
Mouse Orthologue:
Slc2a8
Mouse Description:
solute carrier family 2, (facilitated glucose transporter), member 8 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9411 | Essential Splice Site | Available for shipment | Available now |
sa20575 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9411
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019648 | Essential Splice Site | 256 | 498 | 5 | 10 |
ENSDART00000019648 | Essential Splice Site | 256 | 498 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 68966014)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 65300067 |
GRCz11 | 5 | 65979182 |
KASP Assay ID:
2259-6810.1 (used for ordering genotyping assays)
KASP Sequence:
CCCCGCCGAGTGGGAATGCGCTAGAATAGAAGATGCCTACAAAAATGAAG[T/C]TAGACATCACCAAGTTTTTWGGKTCTTYATTTTATTRAACATAAWGARCT
Long Flanking Sequence:
TTTAAATCTAATGATATAATACAGATAATACAACATTAAGAACAAAGAGAGAGCTCGTCAATCTGTAAAAATGGATAATGTTAAAAAGTGCATTTTGACCAATGAGAGAACAGTTTTGCACACATGACTCGCATGAACACATTTTTAAAAATGTTTTCTTGAAAAATAAAACAGACCAGAAGTTTCAAAACGCAAAGAAATGTTTTGTTTTGAAACTAATCAAATGATTCACAGGTGTAAAAAATGCTCTAAAGTAATGCCAAAGAAATCCTTTCTTCTTTTTTTAGGTTTGTTCCTGGACTGGCGATGGTTAGCAGTGGCATCATCTATTCCTCCCACACTCATGCTGCTGTCCATGTGCTTCATGCCGGAGACGCCACGATTTCTGCTCTGCCAAGGGAAACGGCGGGAAGCAGAGGACGCCCTGCGCTTCCTTAGGGGTCCTGATGCCCCCGCCGAGTGGGAATGCGCTAGAATAGAAGATGCCTACAAAAATGAAG[T/C]TAGACATCACCAAGTTTTTTGGGTCTTCATTTTATTGAACATAATGAACTGCCTTTCAAAATTAAAGTCAGCGTTAAAAGCCTGTTTTAGTTTTTTTAATGTGCCATTTTTTAGTGAACTTGATATTCAGTGAGTTAAAATGTGACATAAAAGAGATTGTTCACCCAAAATTATTTTTAATTAAAACTTATAAATTTCTGTCGAACTGATTTCTCGAACCAGCGACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCACTGCTTCGCCCTGAAATATTGTGTTGTAGGTCTTTAATCATTTTAAACAGGCCCTAATTTCCTTATGTCTTAGTAAAACTAGCCAGTTTTGTTGACACCCAATCATCTACAATTCATCTCCAAACTTTTTATATATATATATATTTAAGTTTTTCATTGCAAAGTGATACAATTCACAACAGCTGTTAGACAACATTTTTACAGCAAATTCTCCAGGGAAAGAAAACTAAAGCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20575
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019648 | Nonsense | 319 | 498 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 68968515)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 65302553 |
GRCz11 | 5 | 65981668 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTTGCCGCAGAGCAGTGATGTGGCCACTGTTATTGTCGCAGCCACA[C/T]AGGTGGTCTTCACTGCAATTGCTGCTCTTATAATGGACAAGGCCGGGCGG
Long Flanking Sequence:
AATTGAAAATTCCATCCTCATTTACTCGCCCTTCACCTGTTTCAAACCTTTATGACTTTCTTTCCCCTGTCGAACACAAAATAAGATAGATCAGCTGGAAACCATCGACTTCCTTAGTATTTGTTTTCACTTGTTTTAAAAGCTTTATGACTTTCTCTCCCTTGTTGAACACAAAGATAGTTTGAAGTAAGCTGGAAACCTGTAACCACTGACTTCCATAGTATTTGTTTTTCCTACTATAAAAAGTCAGTGATTACAAGTTTGCAGCTTTCTTTAAAATATCTTAATCTGTGTTTAATTGAAGAAAGAATGTAATAAAGGTTGGAAATCACTTGAAGGTGAGTAAATTGTCATAATTGGATGAACCATCCCTTTAAGAACAGGGAAAATGTGCTTGAAACACACTTGAAACAGGTCTGACAGGTTTAATAATAAATACCTGTGTCTGTATTTTTTTGCCGCAGAGCAGTGATGTGGCCACTGTTATTGTCGCAGCCACA[C/T]AGGTGGTCTTCACTGCAATTGCTGCTCTTATAATGGACAAGGCCGGGCGGAAAGTTCTTCTCATTTTGTCTGGTAGAAACCTCTTAAAGTCATAATGCATTTGCACCACTTTTATTTGAAGAATTGAAATTGATAATCTGTCATTTTGTGTCCTCAAGGTGTCGTCATGTGTATTAGCGAAGCAGTGTTTGGAGTGTACTTTAAGCTGACTGTGATGAAGCCCAATAACTCCTCATTGACCAGTGTGCTAACGGACACCCATGGTCTTCTGGAAGATCAGCCCTCTGCAGACCTGGCCTGGTTGGCTGTGGGAAGCATGGGCTTTTTCATTGCAGGTTAGAAGGACTGTATTTCTCTGAACAAGAATTATTTAGCAGTACTACTGTATGTCTTTTCAAAGAAAAAATTCTTAAAACAGTTTACATCTTGAATTTGTTCTGTACTTATGTACATTAATATCCATTCAGTGAGCAAACTGCATTTATTCTGACTCATAAGCA
Associated Phenotype:
Not determined